Dissecting Hedgehog, TGF beta and BMP Signaling During Pancreatic Tumorigenesis

剖析胰腺肿瘤发生过程中的 Hedgehog、TGF beta 和 BMP 信号传导

• 批准号: 8034649
• 负责人: BRIAN C LEWIS
• 金额: $ 34.39万
• 依托单位: UNIV OF MASSACHUSETTS MED SCH WORCESTER
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-04-08 至 2016-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8034649
• 关键词: Address; Alleles; American; BMPR2 gene; Biochemical; Biological; Biological Models; Cancer Etiology; Cancer cell line; Cell Culture Techniques; Cell Line; Cells; Cessation of life; Collection; Conflict (Psychology); Data; Defect; Development; Diagnosis; Disease; Disease Progression; Epithelial; Epithelial Cells; Epithelium; Erinaceidae; Event; Family; Frequencies; Gene Expression Profiling; Genes; Genetic; Genetic Transcription; Gli2 protein; In Vitro; KRAS2 gene; Lead; Lesion; Ligands; Malignant Neoplasms; Malignant neoplasm of pancreas; Mediating; Molecular; Mutation; Oncogenes; Pancreas; Pancreatic Ductal Adenocarcinoma; Pathogenesis; Pathway interactions; Phenotype; Phosphotransferases; Primary Cell Cultures; Public Health; Publishing; Relative (related person); Repressor Molecules; Role; Sampling; Signal Pathway; Signal Transduction; Specimen; Transforming Growth Factor beta; Tumor Cell Line; United States; Work; autocrine; bone morphogenetic protein receptors; bone morphogenic protein; cancer cell; cancer initiation; carcinogenesis; cell behavior; in vivo; mortality; mouse model; novel; novel therapeutics; pancreatic cancer cells; pancreatic neoplasm; pancreatic tumorigenesis; paracrine; postnatal; receptor; research study; small hairpin RNA; smoothened signaling pathway; statistics; transcription factor; tumor; tumor progression

DESCRIPTION (provided by applicant): Pancreatic cancer is a leading cause of cancer-related mortality in the United States, with an estimated 35,000 people dying from this disease in 2009. Activating mutations in the KRAS2 oncogene occur in >90% of pancreatic ductal adenocarcinomas (PDAC), the most common type of pancreatic cancer, and are believed to be initiating lesions in PDAC. Elevated levels of hedgehog pathway components are found in a majority of PDAC specimens and cell lines. Loss of the Smad4 transcriptional regulator occurs in approximately half of PDAC cases, and inactivation of the TGF?RII, BMPRII, and ALK4 receptor kinases that act upstream of Smad4 occurs in a smaller subset of PDAC cases. Yet, the precise roles of the hedgehog pathway and the signaling pathways activated by TGF-? family ligands in PDAC remain unclear. This application therefore proposes to use a novel mouse modeling system and complementary cell culture and in vitro studies to systematically investigate the roles of these pathways in pancreatic carcinogenesis. Prior studies have provided conflicting data on whether hedgehog ligands act in both autocrine and paracrine fashion, or only a paracrine manner, during pancreatic tumor development. Therefore, studies in Aim 1 will use novel mouse models to directly compare the ability of sonic hedgehog (Shh) and its downstream transcription factors Gli1 and Gli2 to cooperate with activated Kras during pancreatic tumorigenesis in vivo. Analyses of tumor samples and cell lines generated from the tumors induced in this Aim will be performed to determine whether Shh stimulates signaling in both the cancer cells and the reactive stroma, or only within the reactive stroma. Finally, using a novel dominant-repressor Gli3 allele, the requirement for Gli transcription activity in Kras-induced pancreatic tumorigenesis will be determined. The studies in Aim 2 will identify the relative contributions of defects in TGF-? and BMP signaling to pancreatic tumorigenesis. ShRNAs targeting Smad4, TGF?RII, or BMPRII will be delivered specifically to the pancreatic epithelium in vivo, and their ability to cooperate with activated Kras determined. Complementary experiments in cancer cell lines derived from the induced tumors will be performed to determine whether defects in TGF-( or BMP signaling alter the phenotypes of pancreatic cancer cells, and how TGF-( family ligands influence pancreatic cancer cell behavior. The studies in Aim 3 will determine whether there is cross-talk between the hedgehog and TGF-( signaling cascades in pancreatic cancer cells, and how this cross-talk influences the phenotypes of these cells. Finally, gene expression profiling will be used to identify important genes downstream of the hedgehog and TGF-( signaling cascades. The biological importance of these genes during pancreatic tumorigenesis will be validated using studies of the cancer cell lines generated in Aims 1 and 2, and the ability of these genes to cooperate with activated Kras during pancreatic tumorigenesis in vivo. PUBLIC HEALTH RELEVANCE: Pancreatic cancer claims the lives of 35,000 Americans annually; therefore understanding the mechanisms that contribute to the initiation and progression of this disease is of great significance. Through the use of novel mouse models for pancreatic cancer, this application seeks to understand how alterations in the hedgehog, transforming growth factor beta, and bone morphogenic protein signaling pathways contribute to pancreatic cancer initiation and progression. These studies will significantly enhance the understanding of pancreatic cancer, and may lead to the development of novel therapeutic strategies, thereby reducing the impact of this disease on public health.

描述（由申请人提供）：胰腺癌是美国癌症相关死亡的主要原因，2009年估计有35,000人死于该疾病。KRAS2癌基因的激活突变发生在90%的胰导管腺癌（PDAC）中，这是最常见的胰腺癌类型，并且被认为是PDAC的初始病变。在大多数PDAC标本和细胞系中发现了高水平的刺猬通路成分。Smad4转录调节因子的缺失发生在大约一半的PDAC病例中，TGF？RII， BMPRII和ALK4受体激酶作用于Smad4的上游，出现在PDAC病例的较小子集中。然而，刺猬通路和TGF-激活的信号通路的确切作用？PDAC的家族配体尚不清楚。因此，本应用程序建议使用一种新的小鼠建模系统和互补细胞培养和体外研究来系统地研究这些途径在胰腺癌发生中的作用。